Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908209
rs121908209
TPP1
T 0.700 GeneticVariation CLINVAR [Tripeptidyl peptidase 1 deficiency in neuronal ceroid lipofuscinosis. A novel mutation]. 12698559

2003
dbSNP: rs121908209
rs121908209
TPP1
T 0.700 CausalMutation CLINVAR